-
1
-
-
2742571467
-
-
Harano K., Yasuda M., Ida Y., Komori T., and Taguchi T. Cryst. Struc. Commun. 10 (1981) 165
-
(1981)
Cryst. Struc. Commun.
, vol.10
, pp. 165
-
-
Harano, K.1
Yasuda, M.2
Ida, Y.3
Komori, T.4
Taguchi, T.5
-
6
-
-
0033950253
-
-
Watanabe A., Moriguchi M., Ito F., Yoshitake Y., Eto M., and Harano K. Heterocycles 53 (2000) 1
-
(2000)
Heterocycles
, vol.53
, pp. 1
-
-
Watanabe, A.1
Moriguchi, M.2
Ito, F.3
Yoshitake, Y.4
Eto, M.5
Harano, K.6
-
7
-
-
27944491127
-
-
Ito F., Moriguchi T., Yoshitake Y., Eto M., Yahara S., and Harano K. Chem. Pharm. Bull. 51 (2003) 688
-
(2003)
Chem. Pharm. Bull.
, vol.51
, pp. 688
-
-
Ito, F.1
Moriguchi, T.2
Yoshitake, Y.3
Eto, M.4
Yahara, S.5
Harano, K.6
-
9
-
-
2742512091
-
-
Oki M., Allinger N.L., Eliel E.L., and Wilen S.H. (Eds), John Wiley and Sons, New York
-
In: Oki M., Allinger N.L., Eliel E.L., and Wilen S.H. (Eds). Topics in Stereochemistry Vol. 14 (1983), John Wiley and Sons, New York 47-79
-
(1983)
Topics in Stereochemistry
, vol.14
, pp. 47-79
-
-
-
11
-
-
0000462370
-
-
Cozzi F., Cinquini M., Annunziata R., Dwyer T., and Siegel J.S. J. Am. Chem. Soc. 114 (1992) 5729
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 5729
-
-
Cozzi, F.1
Cinquini, M.2
Annunziata, R.3
Dwyer, T.4
Siegel, J.S.5
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14
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34547129534
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note
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AMI calculations were run through the CS Chem3D Pro interface using MOPAC97 on a Power Macintosh G4 computer.
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15
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85086751741
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note
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2 nature of the amide group of the 1-aroylindoline moiety.
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16
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34547137842
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note
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The colors of the coupling reaction products are summarized as follows. {A figure is presented} The UV-vis spectra of 6 showed long absorption tailings up to 500 nm and the difference spectra gave broad peaks around 420-nm. The molar absorptivities at 420 nm are 205.4 for 6dj, 413.2 for 6eh and 376.6 for 6ej.
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17
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34547114673
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note
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The closest intra- and intermolecular distances between the 4-dimethylaminophenyl and 4-nitrophenyl rings in the crystal structure of 6dj are 3.323 and 3.473, respectively.
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18
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34547138837
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a) Gaussian 98, Revision A.6, M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, V. G. Zakrzewski, J. A. Jr. Montgomery, R. E. Stratmann, J. C. Burant, S. Dapprich, J. M. Millam, A. D. Daniels, K. N. Kudin, M. C. Strain, O. Farkas, J. Tomasi, V. Barone, M. Cossi, R. Cammi, B. Mennucci, C. Pomelli, C. Adamo, S. Clifford, J. Ochterski, G. A. Petersson, P. Y. Ayala, Q. Cui, K. Morokuma, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. Cioslowski, J. V. Ortiz, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, 1. Komaromi, R. Gomperts, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, C. Gonzalez, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, J. L. Andres, C. Gonzalez, M. Head-Gordon, E. S. Replogle, and J. A. Pople. Eds Gaussian: Pittsburgh PA, 1998.
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20
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34547135135
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note
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The DFT TS calculation of 3ab is not easy and is very time-consuming.
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0000514534
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Blackman A., Hambley T.W., Picker R., Taylor W.C., and Thirasana N. Tetrahedron Lett. 28 (1987) 5561
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 5561
-
-
Blackman, A.1
Hambley, T.W.2
Picker, R.3
Taylor, W.C.4
Thirasana, N.5
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23
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0000604488
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SIR92:
-
SIR92:. Altomare A., Cascarano G., Giacovazzo C., Guagliardi A., Burla M., Polidori G., and Camalli M. J. Appl. Cryst. 27 (1994) 435
-
(1994)
J. Appl. Cryst.
, vol.27
, pp. 435
-
-
Altomare, A.1
Cascarano, G.2
Giacovazzo, C.3
Guagliardi, A.4
Burla, M.5
Polidori, G.6
Camalli, M.7
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25
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0004264855
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Issue 10, Chemical Crystallography Laboratory, Oxford, UK
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Issue 10. Watkin D.J., Prout C.K., Carruthers J.R., and Betteridge P.W. CRYSTALS (1996), Chemical Crystallography Laboratory, Oxford, UK
-
(1996)
CRYSTALS
-
-
Watkin, D.J.1
Prout, C.K.2
Carruthers, J.R.3
Betteridge, P.W.4
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